Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2523710
MICB-DT
1.000 0.120 6 31483132 intron variant G/A snv 0.14 1
rs2608053
PVT1
1.000 0.120 8 128063586 intron variant T/C snv 0.50 1
rs4733809
PVT1
1.000 0.120 8 127977046 intron variant C/T snv 0.54 1
rs6439924
LOC105374132 ; CLSTN2
1.000 0.120 3 140450815 intron variant A/C snv 0.21 1
rs7111520
POU2AF1
1.000 0.120 11 111378886 intron variant G/A snv 0.58 1
rs752427
PVT1
1.000 0.120 8 127967762 intron variant C/T snv 0.55 1
rs805286
LY6G6E ; LY6G6D ; LY6G6F-LY6G6D
1.000 0.120 6 31711530 intron variant A/G snv 0.42 1
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs9880772 0.827 0.240 3 27736288 intergenic variant G/A snv 0.59 5
rs9392017 0.851 0.160 6 442357 intergenic variant G/A;C snv 4
rs13195441 0.925 0.200 6 32775521 intergenic variant G/A snv 0.30 2
rs756440 0.925 0.160 6 33154554 intergenic variant A/G snv 0.24 2
rs6565176 1.000 0.120 16 30163605 intergenic variant T/A;C snv 1
rs9267947 1.000 0.120 6 32243441 intergenic variant A/G;T snv 1
rs121964877
CDH1
0.851 0.160 16 68822081 stop gained C/G;T snv 5
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188